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この商品について
化学式:
(CH3)2SO
CAS番号:
分子量:
78.13
UNSPSC Code:
12191502
NACRES:
NA.24
PubChem Substance ID:
EC Number:
200-664-3
Beilstein/REAXYS Number:
506008
MDL number:
製品名
ジメチルスルホキシド, analytical standard
InChI key
IAZDPXIOMUYVGZ-UHFFFAOYSA-N
InChI
1S/C2H6OS/c1-4(2)3/h1-2H3
SMILES string
CS(C)=O
grade
analytical standard
vapor density
2.7 (vs air)
vapor pressure
0.42 mmHg ( 20 °C)
assay
≥99.95% (GC)
autoignition temp.
573 °F
shelf life
limited shelf life, expiry date on the label
expl. lim.
42 %, 63 °F
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
refractive index
n20/D 1.479 (lit.)
n20/D 1.479
bp
189 °C (lit.)
mp
16-19 °C (lit.)
solubility
H2O: miscible (completely)
density
1.10 g/mL (lit.)
application(s)
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
format
neat
Quality Level
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Disclaimer
容易に過冷却状態となり、室温で徐々に再融解します。凝固している場合は室温に放置すると、劣化させることなく液体に戻すことができます。
Application
DMSO may be used as an analytical standard for the determination of the analyte in environmental samples by gas chromatography (GC) technique.
Dimethyl sulfoxide may be used as a molecular probe in the detection and analysis of hydroxyl radicals generated in advanced oxidation processes using high performance liquid chromatography(HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Dimethyl Sulfoxide (DMSO) contains both highly polar and apolar groups, which impart it an amphipathic character. It can dissolve in both aqueous and organic solvents. It is a commonly used solvent in hydrophobic pharmaceutical agents, exhibiting effective hydroxyl radical scavenging ability.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
For information on dimethyl sulfoxide miscibility, please visit the following link:
Dimethyl Sulfoxide Miscibility/Immiscibility Table
Dimethyl Sulfoxide Miscibility/Immiscibility Table
保管分類
10 - Combustible liquids
wgk
WGK 1
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Determination of hydroxyl radicals in advanced oxidation processes with dimethyl sulfoxide trapping and liquid chromatography
Tai C, et al.
Analytica Chimica Acta, 527(1), 73-80 (2004)
Determination of hydroxyl radicals in advanced oxidation processes with dimethyl sulfoxide trapping and liquid chromatography
Tai C, et al.
Analytica Chimica Acta, 527, 73-80 (2004)
Nuno C Santos et al.
Biochemical pharmacology, 65(7), 1035-1041 (2003-03-29)
DMSO is an amphipathic molecule with a highly polar domain and two apolar methyl groups, making it soluble in both aqueous and organic media. It is one of the most common solvents for the in vivo administration of several water-insoluble
Lead-free halide perovskite solar cells with high photocurrents realized through vacancy modulation.
Mulmudi Hemant Kumar et al.
Advanced materials (Deerfield Beach, Fla.), 26(41), 7122-7127 (2014-09-13)
Lead free perovskite solar cells based on a CsSnI3 light absorber with a spectral response from 950 nm is demonstrated. The high photocurrents noted in the system are a consequence of SnF2 addition which reduces defect concentrations and hence the
Björn Zörner et al.
Brain : a journal of neurology, 137(Pt 6), 1716-1732 (2014-04-17)
Anatomical plasticity such as fibre growth and the formation of new connections in the cortex and spinal cord is one known mechanism mediating functional recovery after damage to the central nervous system. Little is known about anatomical plasticity in the
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